We undertake microbiological investigations of quality control throughout the entire life cycle of medicinal products. The European Pharmacopoeia (EuAB) sets requirements for the microbiological quality of prescription drugs which must be fulfilled in order to obtain approval for registration.
Similarily, there are microbiological quality standards for over-the-counter drugs and medical devices (container, applications systems). Suitable data have to be presented to the regulatory bodies (TÜV).
We have a long experience in providing appropriate data for the registration of nasal and ophthalmic medications.
Testing of the efficacy of preservatives used in pharmaceuticals
Testing of the microbiological quality of medications with and without preservatives
Testing of the microbiological safety of medicinal products
Investigation of the microbiological stability of products (shelf life) during simulation models